@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_head
{
this:
np:hasAssertion
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion
;
np:hasProvenance
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion
a
np:Assertion
.
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_provenance
a
np:Provenance
.
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0232197
a
ncit:C7057
.
dgn-gda:DGN37f7cb65c5623422765ec47af10e84f1
sio:SIO_000628
miriam-gene:6331
,
lld:C0232197
;
a
sio:SIO_001121
.
}
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_provenance
{
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_assertion
dcterms:description
"[Mutations in SCN5A, the gene encoding Na(v)1.5, have been linked to many cardiac phenotypes, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus syndrome, atrial fibrillation, and dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19744495
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP762496.RAd1BHz6FQElQdWL1mRB8AoiiBqP5p3MkO971b4949nvs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:30+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}